CN107300544B - Detection method of ferrous ions - Google Patents
Detection method of ferrous ions Download PDFInfo
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- CN107300544B CN107300544B CN201710459300.XA CN201710459300A CN107300544B CN 107300544 B CN107300544 B CN 107300544B CN 201710459300 A CN201710459300 A CN 201710459300A CN 107300544 B CN107300544 B CN 107300544B
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/6428—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/6428—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
- G01N21/643—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" non-biological material
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/6428—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
- G01N2021/6432—Quenching
Abstract
The invention discloses a detection method of ferrous ions, which uses a carbon quantum dot-manganese dioxide composite material as a fluorescent probe to detect the ferrous ions, adds the ferrous ions with different concentrations into the carbon quantum dot-manganese dioxide composite material, measures the fluorescence intensity of the ferrous ions, and then uses the fluorescence rise intensity delta F to map the concentration of the added ferrous ions to obtain a linear equation of delta F-20.5 +228.7[ Fe ]2+]Linear correlation coefficient R thereof2Is 0.996, the detection limit of the detection method is as low as 0.17 mu M, and the detection method is used for Fe2+Has good selectivity and can eliminate the interference of other metal ions. Compared with the prior art, the detection method of ferrous ions disclosed by the invention has the advantages of simplicity, practicability, reliability and the like, and can be widely applied to practice.
Description
Technical Field
The invention relates to a method for detecting ferrous ions, in particular to a method for detecting ferrous ions by taking a carbon quantum dot-manganese dioxide composite material as a fluorescent probe.
Background
Iron is a common element in nature and is one of the most active elements in water environments. In addition, iron is widely present in human bodies, animal and plant bodies, food and medicine, is an indispensable trace element for human bodies, plays a vital role for human bodies, and has toxic and potential harm to human bodies due to excessive intake of iron, for example, iron participates in oxygen transportation, formation of a plurality of coenzymes, maintenance of hematopoietic function, enhancement of immune function and the like. The method has important significance in establishing a rapid and accurate method for determining the content of iron in the environmental water sample.
At present, three main types of methods for measuring iron exist. First, inductively coupled plasma emission spectroscopy, ICP-AES, is a low detection limit and high accuracy method, but this method is expensive and can only measure total iron ions. Secondly, atomic absorption, the method and ICP-AES have the same disadvantages, and the sample pretreatment is complicated. Third, spectrophotometry.
Disclosure of Invention
The invention provides a method for detecting ferrous ions, which takes a carbon quantum dot-manganese dioxide composite material as a fluorescent probe to realize high-sensitivity quantitative detection of the ferrous ions.
The technical scheme adopted by the invention is as follows:
a detection method of ferrous ions uses a carbon quantum dot-manganese dioxide composite material as a fluorescent probe to detect the ferrous ions.
The detection method comprises the following steps:
(1) preparing a carbon quantum dot-manganese dioxide composite material;
(2) diluting the carbon quantum dot-manganese dioxide composite material obtained in the step (1) by 10 times, then adding ferrous ions with different concentrations, adjusting the pH of the system to 4.4-5.5, and testing the fluorescence spectrum of the system;
(3) in a rectangular coordinate system, the fluorescence rise-back intensity delta F is used for plotting the concentration of the added ferrous ions, curve fitting is carried out to obtain a linear equation, and the corresponding Fe under any fluorescence rise-back intensity can be calculated according to the linear equation2+Wherein Δ F ═ F-F0，F0To add no Fe2+The fluorescence intensity of the system at the wavelength of 450nm, F is added with Fe2+The fluorescence intensity at a wavelength of 450nm is plotted.
The linear equation is Δ F ═ 20.5+228.7[ Fe [ ]2+]Linear correlation coefficient R thereof20.996, detection limit 0.17. mu.M; and has good linear relation in the range of 0-3.5 mu M.
In the step (2), the final concentration of ferrous ions is 0, 0.15 μ M, 0.3 μ M, 0.75 μ M, 1.0 μ M, 1.25 μ M, 1.5 μ M, 1.75 μ M, 2.0 μ M, 2.25 μ M, 2.5 μ M, 3.0 μ M, 3.5 μ M in sequence.
Further, in the step (2), the pH of the system is adjusted to 4.8.
The preparation method of the carbon quantum dot-manganese dioxide composite material comprises the following steps:
(1-1) preparing carbon quantum dots: dissolving citric acid and ethylenediamine in deionized water, preparing a brownish black product by adopting a hydrothermal method, filling the product into a dialysis bag, and dialyzing in distilled water to obtain a carbon quantum dot solution;
(1-2) preparing a manganese dioxide nanosheet solution: after completely mixing hydrogen peroxide and tetramethylammonium hydroxide pentahydrate, quickly adding the hydrogen peroxide and the tetramethylammonium hydroxide pentahydrate into a manganese dichloride tetrahydrate solution, stirring and reacting for 8 hours, and washing a product by using ethanol and deionized water in sequence; dispersing the washed product in deionized water to prepare a manganese dioxide nanosheet solution with the concentration of 220 mu M;
and (1-3) adding the carbon quantum dot solution obtained in the step (1-1) into the manganese dioxide nanosheet solution obtained in the step (1-2) according to the volume ratio of 1:1, and thus obtaining the carbon quantum dot-manganese dioxide composite material.
In the step (1-1), the ratio of citric acid: ethylene diamine: deionized water 1.05 g: 335 μ L: 10 mL; the temperature of the hydrothermal reaction is 200 ℃ and the time is 5 h.
In the step (1-1), the cut-off molecular weight of the dialysis bag is 3000 Da; the volume of the distilled water is 150-200 mL, and the dialysis time is 4-5 hours.
The step (1-2) specifically comprises: 2mL of 30% H by mass2O2Adding the mixture into 12mL of tetramethylammonium hydroxide pentahydrate with the concentration of 1mol/L, quickly adding the mixture into 10mL of manganese dichloride tetrahydrate solution with the concentration of 0.3mol/L after completely mixing, quickly changing the solution into dark brown, continuously stirring for 8 hours, washing the product by using 95% ethanol and deionized water in sequence, filtering, and dispersing the product in the deionized water to prepare manganese dioxide solution with the concentration of 220 MuM.
The detection method can eliminate the interference of other metal ions. The other metal ion is Co2+、Ni2+、Zn2+、Na+、Cu2+、Mg2+、Ca2+、Cd2+、K+And Al3+。
The invention discloses a method for detecting ferrous ions, which uses citric acid as a carbon source to prepare carbon quantum dots with strong fluorescence by a hydrothermal method, and constructs a rapid detection method for Fe by using a fluorescence quenching-rising mechanism of the carbon quantum dots (CDs)2+The method of (1). Firstly, using citric acid as a carbon source to prepare CDs by a hydrothermal method, and then adding the CDs into manganese dioxide (MnO)2) In nano-flakes, by internal light filtering effectQuenching the fluorescence of CDs to form CDs-MnO2And (3) a probe. When Fe is added to the probe2+Due to MnO2Will react with Fe2+Oxidation-reduction reaction occurs to thereby make MnO2Dissolving the nano-flake to generate Mn2+Ions, thereby recovering the fluorescence of CDs and increasing the fluorescence and Fe under certain conditions2+The ion concentration is directly proportional.
The invention is based on MnO2The nanosheets quench the fluorescence of the CDs. And Fe2+Can be associated with MnO2Oxidation-reduction reaction of the nanosheet, thereby rendering MnO2Dissolving the nano-flake to generate Mn2+Ions, resulting in fluorescence back-up of the CDs. The detection limit of the detection method is as low as 0.17 mu M, and the detection method is used for Fe2+Has good selectivity and can eliminate the interference of other metal ions.
Compared with the prior art, the detection method of ferrous ions disclosed by the invention has the advantages of simplicity, practicability, reliability and the like, can be widely applied to practice, and is used for detecting Fe with high sensitivity and low cost in the future research2+The probe provides a new idea.
Drawings
FIG. 1 is a schematic diagram of the synthesis of a carbon quantum dot-manganese dioxide composite;
FIG. 2 shows CDs (A), MnO2Transmission electron microscope images of the nano-sheet (B) and the carbon quantum dot-manganese dioxide composite material (C);
FIG. 3 shows CDs-MnO2Adding Fe with different concentrations into the system2+(from the top down Fe)2+The concentration of (A) is as follows: 0-3.5 μ M) fluorescence spectrum;
FIG. 4 shows fluorescence rising intensity Δ F and Fe2+A linear plot of concentration;
FIG. 5 shows CDs-MnO2The selectivity experiment chart of the system to ferrous ions;
FIG. 6 shows MnO2Concentration of nanosheet to CDs-MnO2System for detecting Fe2+The influence of (a);
FIG. 7 is pH vs. CDs-MnO for the system2System for detecting Fe2+The influence of (c).
Detailed Description
Example 1
A detection method of ferrous ions comprises the following steps:
(1) preparing a carbon quantum dot-manganese dioxide composite material, wherein the synthetic schematic diagram is shown in figure 1;
(1-1) weighing 1.05g of citric acid and 335 mu L of ethylenediamine, dissolving in 10mL of deionized water, fully stirring to completely dissolve, transferring the solution to a polytetrafluoroethylene-high pressure reaction kettle with the volume of 30mL, heating at 200 ℃ for 5h, naturally cooling to room temperature after the reaction is finished to obtain a brownish black product, filling the product into a dialysis bag with the molecular weight cutoff of 3000Da, sealing, putting the dialysis bag into 150-200 mL of deionized water for dialysis for 4-5 hours, collecting the dialyzate to obtain a CDs solution, and putting the CDs solution into a refrigerator for refrigeration for later use. The transmission electron microscope image is shown in FIG. 2A, and the particle size of CDs is 2-4 nm, and the dispersity is good;
(1-2) 2mL of 30% by mass H2O2Adding the mixture into 12mL of tetramethylammonium hydroxide pentahydrate with the concentration of 1mol/L, quickly adding the mixture into 10mL of manganese dichloride tetrahydrate solution with the concentration of 0.3mol/L after complete mixing, quickly changing the solution into dark brown, continuously stirring for 8 hours, washing the product by using 95% ethanol and deionized water in sequence, filtering to obtain a black solid product, dispersing the black solid product in the deionized water, and obtaining uniformly dispersed manganese dioxide nanosheet solution with the concentration of 220 MuM by utilizing ultrasonic dispersion. The transmission electron micrograph is shown in FIG. 2B, from which MnO can be seen2The nano-sheets are very pure, have better shapes and are uniformly dispersed;
(1-3) mixing the carbon quantum dot solution obtained in the step (1-1) according to a volume ratio of 1: and 1, adding the mixture into the manganese dioxide nanosheet solution obtained in the step (1-2), and stirring and mixing uniformly to obtain the carbon quantum dot-manganese dioxide composite material. The transmission electron micrograph is shown in FIG. 2C, from which it can be seen that CDs have adhered to MnO2The surface of the nano-sheet shows carbon quantum dot-manganese dioxide (CDs-MnO)2) Fluorescent probes of composite materials have been synthesized.
(2) Diluting the carbon quantum dot-manganese dioxide composite material obtained in the step (1)Releasing by 10 times, wherein the concentration of the manganese dioxide nanosheets in the solution is 11 mu M, then adding ferrous ions with different concentrations, adjusting the pH of the system to be 4.8 by using PBS buffer solution, and sequentially adjusting the final concentrations of the ferrous ions as follows: 0. 0.15. mu.M, 0.3. mu.M, 0.75. mu.M, 1.0. mu.M, 1.25. mu.M, 1.5. mu.M, 1.75. mu.M, 2.0. mu.M, 2.25. mu.M, 2.5. mu.M, 3.0. mu.M, 3.5. mu.M, and the fluorescence spectrum of the system was measured, and the obtained fluorescence spectrum was shown in FIG. 3, from which it can be seen that with Fe2+The fluorescence intensity of the system is gradually enhanced by the gradual increase of the concentration.
(3) In a rectangular coordinate system, the fluorescence rise-back intensity Δ F is plotted against the concentration of added ferrous ions, and curve fitting is performed, as shown in FIG. 4, from which it can be seen that Δ F and [ Fe ] are within the range of 0-3.5 μ M2+]Exhibits good linearity, and obtains a linear equation of-20.5 +228.7[ Fe ═ F2+]Linear correlation coefficient R thereof20.996, the detection limit is 0.17 mu M, and the corresponding Fe under any fluorescence rise-back intensity can be calculated according to a linear equation2+Wherein Δ F ═ F-F0，F0To add no Fe2+The fluorescence intensity of the system at the wavelength of 450nm, F is added with Fe2+The fluorescence intensity at a wavelength of 450nm is plotted.
Example 2
Selectivity test
Co was added to the carbon quantum dot-manganese dioxide composite material obtained in step (1) in example 1 at the same concentration2+、Ni2+、Zn2+、Na+、Cu2+、Mg2+、Ca2+、Cd2+、K+And Al3+Measuring the fluorescence intensity, and taking Δ F as ordinate and ion species as abscissa to make bar chart, and then adding Fe into the system containing these ions respectively2+The fluorescence intensity was measured and plotted as a histogram with Δ F as ordinate and ion species as abscissa, in this experiment, other metal ions (Co)2+、Ni2+、Zn2+、Na+、Cu2+、Mg2+、Ca2+、Cd2+、K+And Al3+) Has a final concentration of 2.0. mu. mol/L, Fe2+The final concentration of (2.0. mu. mol/L) was determined, and the other experimental conditions were the same as in example 1.
The results are shown in FIG. 5, which shows that the results are for CDs-MnO2When other metal ions with the same concentration are added into the system, the other metal ions are opposite to CDs-MnO2The fluorescent intensity of the system is basically not influenced by the rise. However, when continuing to add Fe to the system2+When the fluorescence intensity of the system rises, the fluorescence intensity of the system rises. The results demonstrate CDs-MnO2System used as fluorescent sensor for detecting Fe2+Has very good selectivity and specificity, so the method can be used for quantitatively detecting Fe in a solution2+The content of (a).
Example 3
MnO2Concentration of nanosheet vs. Fe2+Influence of detection
To contain different MnO2CDs-MnO with nanosheet concentration2Adding Fe with final concentration of 1 mu M into the composite material2+The fluorescence intensity was measured under the same other experimental conditions as in example 1, and Δ F was taken as the ordinate, MnO2The final concentration of the nanoplatelets is plotted on the abscissa, as shown in FIG. 6, from which it can be seen that MnO2When the concentration of the nanosheets is very low, the fluorescence rise of the CDs is low; when MnO is not yet present2Too high a concentration of nanoplatelets inhibits the fluorescence rise of CDs due to Fe in the solution2+Can react with free MnO2The nanosheets react, thereby hindering CDs from MnO2And (4) combining the nano sheets. Based on the above two factors, MnO2The optimum concentration of nanoplatelets is 11 μ M.
Example 4
System pH vs. Fe2+Influence of detection
To CDs-MnO of different pH values2Adding Fe with the final concentration of 1 mu M into a fluorescent probe system of the composite material2+In other experimental conditions, the fluorescence intensity was measured as in example 1, and a graph was plotted with Δ F as the ordinate and the system pH as the abscissa, as shown in fig. 7, in which the Δ F value of the system gradually increased in the pH range of 3.5 to 4.8 and reached the highest point of the peak at pH 4.8. This is because the fluorescence intensity of CDs is lower at lower pH valuesWill be weakened and will affect the detection effect. When the pH is greater than 4.8, Δ F decreases. This is probably due to Fe with increasing pH2+Hydrolysis may occur.
The above detailed description of a method for detecting ferrous ions with reference to the embodiments is illustrative and not restrictive, and several embodiments can be enumerated within the scope of the limitations, so that variations and modifications thereof can be included within the scope of the present invention without departing from the general concept of the present invention.
Claims (5)
1. The detection method of the ferrous ions is characterized in that the detection method uses a carbon quantum dot-manganese dioxide composite material as a fluorescent probe to detect the ferrous ions;
the detection method comprises the following steps:
(1) preparing a carbon quantum dot-manganese dioxide composite material;
(2) diluting the carbon quantum dot-manganese dioxide composite material obtained in the step (1) by 10 times, then adding ferrous ions with different concentrations, adjusting the pH of the system to 4.4 ~ 5.5.5, and testing the fluorescence spectrum of the system;
(3) in a rectangular coordinate system, the fluorescence rise-back intensity delta F is used for plotting the concentration of the added ferrous ions, curve fitting is carried out to obtain a linear equation, and the corresponding Fe under any fluorescence rise-back intensity can be calculated according to the linear equation2+Wherein Δ F = F-F0，F0To add no Fe2+The fluorescence intensity of the system at the wavelength of 450nm, F is added with Fe2+The fluorescence intensity of the system at a wavelength of 450 nm;
the preparation method of the carbon quantum dot-manganese dioxide composite material comprises the following steps:
(1-1) preparing carbon quantum dots, namely weighing 1.05g of citric acid and 335 mu L of ethylenediamine, dissolving the citric acid and the ethylenediamine in 10mL of deionized water, fully stirring to completely dissolve the citric acid and the ethylenediamine, transferring the solution to a polytetrafluoroethylene-high-pressure reaction kettle with the volume of 30mL, heating the solution at 200 ℃ for 5 hours, naturally cooling the solution to room temperature after the reaction is finished to obtain a brownish black product, filling the product into a dialysis bag with the molecular weight cutoff of 3000Da, sealing the dialysis bag, dialyzing the dialysis bag in 150mL of ~ 200mL of deionized water for 4 ~ 5 hours, and collecting dialysate to obtain a CDs solution;
(1-2) 2mL of 30% by mass H2O2Adding the mixture into 12mL of tetramethylammonium hydroxide pentahydrate with the concentration of 1mol/L, quickly adding the mixture into 10mL of manganese dichloride tetrahydrate solution with the concentration of 0.3mol/L after complete mixing, quickly changing the solution into dark brown, continuously stirring for 8 hours, washing the product by using 95% ethanol and deionized water in sequence, filtering to obtain a black solid product, dispersing the black solid product in the deionized water, and obtaining uniformly dispersed manganese dioxide nanosheet solution with the concentration of 220 mu M by utilizing ultrasonic dispersion;
(1-3) mixing the carbon quantum dot solution obtained in the step (1-1) according to a volume ratio of 1: and 1, adding the mixture into the manganese dioxide nanosheet solution obtained in the step (1-2), and stirring and mixing uniformly to obtain the carbon quantum dot-manganese dioxide composite material.
2. The detection method according to claim 1, wherein the linear equation is Δ F = -20.5+228.7[ Fe2+]Linear correlation coefficient R thereof20.996, detection limit 0.17. mu.M.
3. The detection method according to claim 1, wherein in the step (2), the final concentration of ferrous ions is 0, 0.15 μ M, 0.3 μ M, 0.75 μ M, 1.0 μ M, 1.25 μ M, 1.5 μ M, 1.75 μ M, 2.0 μ M, 2.25 μ M, 2.5 μ M, 3.0 μ M, 3.5 μ M in this order.
4. The detection method according to any one of claims 1 to 3, wherein in the step (2), the pH of the system is adjusted to 4.8.
5. The detection method according to claim 1, wherein the detection method can exclude interference of other metal ions, wherein the other metal ions are Co2+、Ni2+、Zn2+、Na+、Cu2+、Mg2+、Ca2+、Cd2+、K+And Al3+。
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| CN109975253B (en) * | 2017-12-27 | 2022-05-31 | 中国科学院宁波材料技术与工程研究所 | Fluorescent indicator composition, fluorescent array sensor, preparation method and application thereof |
| CN108760702B (en) * | 2018-05-29 | 2021-08-27 | 安徽师范大学 | Detection method of sulfide ions |
| CN108760701B (en) * | 2018-05-29 | 2022-02-15 | 安徽师范大学 | Carbon quantum dot using sunflower seed shells as carbon source, preparation method thereof and application thereof in detection of sulfur ions |
| CN109946255B (en) * | 2019-04-09 | 2021-04-09 | 中国科学院电子学研究所 | Arsenic ion detection method |
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